| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:38157429-38157473 | Rare:12 | ||||
| chr12:39315752-39315952 | Common:1; Rare:52 | ||||
| chr12:39333269-39333441 | Common:1; Rare:42 | ||||
| chr12:39538693-39538776 | Rare:27 | ||||
| chr12:40443832-40443987 | Common:2; Rare:25 | ||||
| chr12:41280498-41280723 | Common:2; Rare:47 | ||||
| chr12:42388414-42388557 | Common:2; Rare:16 | ||||
| chr12:44948758-44948927 | Common:1; Rare:33 | ||||
| chr12:45388050-45388298 | Rare:65; Clinvar (benign):1 | ||||
| chr12:45457740-45457820 | Rare:16 | ||||
| chr12:45727440-45727818 | Rare:155 | ||||
| chr12:45959347-45959350 | |||||
| chr12:46383148-46383491 | Common:1; Rare:135 | ||||
| chr12:46383930-46384031 | Rare:27 | ||||
| chr12:46698580-46698710 | Common:1; Rare:15 |